- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06767865
Online Diabetes Clinic Support Program
January 5, 2025 updated by: Dilek Büyükkaya Besen
Online Diabetes Clinic Support Program for Type 2 Diabetic Individuals New to Insulin Therapy
This study highlights the potential of online diabetes clinic support programs in improving treatment adherence, reducing treatment-related anxiety, and enhancing self-management skills in insulin therapy.
Telehealth interventions play a crucial role in optimizing diabetes care and supporting patients in managing their insulin treatment effectively.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study was conducted to examine the effects of the online diabetes polyclinic continuous support program applied to individuals with type 2 diabetes who had just started insulin treatment on patient outcomes (metabolic, psychological and social parameters).
The study was designed as a randomized controlled trial.
It was conducted with 35 individuals in the experimental group who had just started insulin treatment and 32 individuals in the control group.
Individuals were assessed with the individual diagnosis form, hypoglycemic confidence scale, hypoglycemia fear scale, diabetes empowerment scale short form, psychological insulin resistance scale, insulin treatment evaluation scale, perceived social support scale and diabetes history (treatment changes, HbA1c, lipid levels, frequency of hypoglycemia and hyperglycemia, frequency of emergency and hospital visits) before the intervention and in the 3rd and 6th months after the intervention.
Individuals in the experimental group received online training and were subsequently provided with continuous follow-up, counseling, motivation and information-providing message support for three months.
In addition, patients were given a target board containing a daily diabetes management program and were asked to use it for three months.
As a result, it was determined that the online polyclinic service reduced the frequency of hypoglycemia and hyperglycemia in individuals who had just started insulin treatment and reduced emergency room visits (p<0.001).
It was determined that it caused a significant decrease in the HbA1c and lipid levels of the patients in the experimental group and contributed to the cessation of insulin treatment under the supervision of a physician.
It was determined that the online diabetes polyclinic continuous support program was effective in reducing hypoglycemia fear and psychological insulin resistance, and increased hypoglycemic confidence and empowerment levels (p<0.001).
The study showed the potential of the online diabetes polyclinic continuous support initiative in improving the treatment process in patients who had just started insulin.
These results reveal that online support systems can be effective in increasing patients' compliance with treatment and in better managing the treatment process.
Online support has been shown to improve adherence to insulin therapy by providing patients with faster access to information, reduced anxiety about treatment, and greater self-management skills.
This suggests that telehealth and online support programs may play an important role in diabetes management and insulin therapy acceptance.
Study Type
Interventional
Enrollment (Actual)
67
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Alsancak
-
Izmir, Alsancak, Turkey, 35000
- Dokuz Eylül University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Individuals aged 18 and over,
- able to communicate in Turkish,
- diagnosed with type 2 diabetes,
- newly started insulin treatment,
- having and using information technology products (telephone, computer)
- willing to participate in the study voluntarily were included in the study.
Exclusion Criteria:
- Individuals with visual,
- auditory or cognitive impairments,
- a condition that prevents communication,
- cannot use information technology products,
- individuals who do not meet the inclusion criteria
- those who do not agree to participate in the study were not included.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
intervention+ Follow-up at 0-3-6 months
|
Individuals in the experimental group received online training and were subsequently provided with continuous follow-up, counseling, motivation and informative message support for three months.
In addition, patients were given a target board containing a daily diabetes management program and were asked to use it for three months.
|
|
No Intervention: Control Group
Follow-up at 0-3-6 months
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hypoglycemic Confidence Scale
Time Frame: 1 month
|
The Hypoglycemic Confidence Scale is a nine-item self-report scale developed by William Polonsky and colleagues in 2017 that examines the degree to which diabetic patients feel confident and comfortable about their ability to avoid hypoglycemia-related problems.
It was developed for use in adults with diabetes (Type 1 and Type 2 who use insulin).
The Hypoglycemic Confidence Scale focuses on three areas: 1. Self-confidence (e.g., confidence in recognizing and managing hypoglycemia before blood sugar drops too low) 2. Confidence in avoiding hypoglycemia at critical times (e.g., while driving, exercising, and sleeping) 3. Estimation of spouse/partner's confidence.
The Hypoglycemic Confidence Scale items are scored between 1-4 (1; Not at all confident 2; Somewhat confident 3; Moderately confident 4; Very confident).
The ninth scale item for diabetic individuals with a spouse is interpreted as: 1; Not at all confident 2; Somewhat confident 3; Moderately confident 4; Very confident.
|
1 month
|
|
Hypoglycemia Fear Survey (HFS):
Time Frame: 1 month
|
The Hypoglycemia Fear Survey- HFS, was used to determine the fear of hypoglycemia in diabetic individuals.
This scale consists of two subgroups, behavior and anxiety, and a total of 33 items.
The behavior subgroup of this scale consists of 15 items.
In the behavior subgroup; diabetic individuals are asked about what they have done in their daily lives to prevent their blood glucose levels from falling in the last 6 months.
The anxiety subgroup consists of 18 items, and individuals are asked how often they have worried about the items given due to the decrease in their blood glucose levels in the last 6 months.
The answers range from; "0 points: never; 1 point: rarely; 2 points: sometimes; 3 points often; 4 points: always".
The high score obtained indicates that the fear of hypoglycemia is high.
The Turkish validity and reliability were made by Özgül Erol.
|
1 month
|
|
Diabetes Empowerment Scale (DES-Short Form):
Time Frame: 1 month
|
The validity and reliability of the scale were made in 2020.
DES-SF was designed to assess the empowerment levels of individuals regarding their health status.
The scale is a five-point Likert type and has eight items (scored between "Strongly disagree" = 1 and "Strongly agree = 5").
The scale does not have a cut-off score.
The scale is calculated based on the average score.
An increase in the average score indicates an increase in the empowerment level.
|
1 month
|
|
Psychological Insulin Resistance Scale (PIRS)
Time Frame: 1 month
|
The scale was developed by Song and colleagues in 2016.
The scale, which is a 5-point Likert type (1: strongly agree, 2: agree, 3: undecided, 4: disagree, 5: strongly disagree), consists of 18 items and 2 sub-dimensions (Supportive factor and Psycho-cognitive/physical factor).
The total score of the scale varies between 18-90.
A high score obtained from the scale indicates that the patient's psychological resistance to insulin use is high.
The scale was developed by Işık and Colleagues in 2021.
As a result of the Turkish validity and reliability analysis, the scale consists of 12 items and 3 sub-dimensions (supportive, psycho-cognitive, physical factors).
Cronbach's alpha coefficient was determined as 0.82.
|
1 month
|
|
Insulin Therapy Assessment Scale (ITAS)
Time Frame: 1 month
|
The scale was developed by Sürücü et al. in 2017.
Number of sub-dimensions and items: It consists of two sub-dimensions and a total of 20 items.
Positive attitude (4 items): Items 3, 8, 17 and 19; Negative attitude (16 items): Items 1, 2, 4, 5, 6, 7, 9, 10, 11, 12, 13, 14, 15, 16, 18 and 20.
Scale items are rated on a Likert type scale between "strongly disagree" and "strongly agree" and 5 points.
The sum of four positively worded items (4-20) gives the positive evaluation sub-dimension, and the sum of 16 negatively worded items (16-80) gives the negative evaluation sub-dimension.
The sum of the items (20 items) gives the total score (20-100).
The scale total score is found by reversing the four positively worded items and summing them with the other 16 negatively worded items.
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Dilek D Büyükkaya Besen, PhD, Dokuz Eylül University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2023
Primary Completion (Actual)
October 1, 2024
Study Completion (Actual)
October 1, 2024
Study Registration Dates
First Submitted
December 30, 2024
First Submitted That Met QC Criteria
January 5, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 5, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DokuzEU-IHH-DBB-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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